drugset / Trial / NCT01983124
Vemurafenib + Fotemustine to Treat Advanced Melanoma Patients With V600BRAF Mutation Recurred While on Vemurafenib
Phase 2
Completed
31 enrolled
Paola Queirolo
Istituto Nazionale per lo Studio e la Cura dei Tumori · collab
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to evaluate the activity of Vemurafenib in combination with Fotemustine in Patients with unresectable Stage IV melanoma harboring V600 BRAF mutation who recurred while in treatment with Vemurafenib. In addition the feasibility and safety profile of prolonging treatment of this drugs combination will be assessed.
Timeline
- Start
- 2013-02
- Primary completion
- 2014-04
- Completion
- 2015-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vemurafenib | Small molecule | 480 mg | Oral |
| Subject | Vemurafenib | Small molecule | 720 mg | Oral |
| Subject | Vemurafenib | Small molecule | 960 mg | Oral |
| Subject | fotemustine | Small molecule | 100 mg/m2 | Intravenous |